Senior Validation Engineer

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Hillerød

Are you an experienced Validation Engineer or Validation Lead ready to share your knowledge to support our production capacity expansion? Do you have experience of automating processes, without compromising on product quality or are you a newly graduate interesting in processes, documentation and quality? Would you like to join a truly international team, with great colleagues having fun while supporting production sites all over the world? Then apply today! The position As our Senior Validation Engineer you will be in charge of development and implementation projects for new packaging production capacities both for our new and marketed products, across multiple geographical locations. You will become a key member of the project and you will:
  • Lead and contribute to validation activities of the project, from basic design and establishing User Requirement Specification (URS) through to process risk assessment and validation (PV) of new production lines.
  • Align local validation practices to ensure the level of standardisation needed to implement multiple lines at different sites are both Lean and conform with our corporate risk-based validation approach.
  • Be engaged in innovative validation practices, such as remote Factory Acceptance Test (FAT), leveraging validation activities and implementation of ongoing process verification.
    • In return you can look forward to a rich professional experience with strong collaboration with multiple stakeholders from Corporate to local sites, R&D, Production, Suppliers and Quality Assurance (QA) including travel opportunities. Qualifications For this role, we are looking forward to connecting with candidates who:
  • Hold at least a bachelor’s degree in engineering, pharmacy, science or any other relevant field.
  • Have a strong quality mindset combined with experience within drug or device development
  • Have expert knowledge and hands-on experience with quality risk management and validation in medical device manufacturing
  • Have a minimum of 3-5 years of experience as Process or Validation Engineer within a regulated industry (pharmaceutical, medical devices, food…) and understanding of science and technical aspects of the manufacturing processes.
  • Are fluent in English (both written and spoken) and experienced with MS Office 365, Teams, e-TIMS and other relevant software solutions.
    • It would be considered as an advantage if you have a previous experience in a pharmaceutical or medical devices industry either from previous positions or internships. Who are you as a person? Although we try not to place people in boxes, there are some traits that we believe will help you thrive in this role. You are ideally well organised, someone who never compromises on quality and have a pragmatic approach in your work. An innovative thinker, you are willing to act as lead in our lean activities and to challenge the status quo. Patience, strong communicative aptitudes, and stellar stakeholder management skills will help you deal with the local sites and their practices. It is essential that you are a true team-player at heart: you like to collaborate with colleagues and stakeholders in order to achieve common goals. About the department You will join Device Manufacturing Development (DMD) and the Packaging department. We are a key function, bridging Packaging R&D to production. We are involved in the development of new products, and responsible of the development and implementation of manufacturing capacity worldwide for new and marketed products. We have an end-to-end presence from product development to production implementation and support. We are engaged in numerous complex and strategic projects for Novo Nordisk, impacting the company ability to deliver product to the patients, compliance and licence to operate, as well as establishment of the factory of the future globally. Our department located in Hillerød includes 30+ highly engaged skilled professionals from project managers, specialists, validation, process and science experts. We are collaborating with multiple stakeholders and striving for excellence in project execution, science engineering, innovation and technology. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, contact Hans Kristian Rømer West at +45 3079 6795. Deadline 24 October 2023. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 3.10.2023, men kan have været deaktiveret og genaktiveret igen.

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